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166 related items for PubMed ID: 19107781

  • 21. Associations between common variants in the MDR1 (ABCB1) gene and ulcerative colitis among North Indians.
    Juyal G, Midha V, Amre D, Sood A, Seidman E, Thelma BK.
    Pharmacogenet Genomics; 2009 Jan; 19(1):77-85. PubMed ID: 19005421
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  • 22. Two independent genetic factors responsible for the associations of the IBD5 locus with Crohn's disease in the Czech population.
    Hradsky O, Dusatkova P, Lenicek M, Bronsky J, Duricova D, Nevoral J, Vitek L, Lukas M, Cinek O.
    Inflamm Bowel Dis; 2011 Jul; 17(7):1523-9. PubMed ID: 21674708
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  • 23. NELL1, NCF4, and FAM92B genes are not major susceptibility genes for Crohn's disease in Canadian children and young adults.
    Amre DK, Mack DR, Israel D, Krupoves A, Costea I, Lambrette P, Grimard G, Dong J, Levy E.
    Inflamm Bowel Dis; 2012 Mar; 18(3):529-35. PubMed ID: 21472827
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  • 24. Genome-wide association study signal at the 12q12 locus for Crohn's disease may represent associations with the MUC19 gene.
    Kumar V, Mack DR, Marcil V, Israel D, Krupoves A, Costea I, Lambrette P, Grimard G, Dong J, Seidman EG, Amre DK, Levy E.
    Inflamm Bowel Dis; 2013 May; 19(6):1254-9. PubMed ID: 23619718
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  • 25. Epistasis between Toll-like receptor-9 polymorphisms and variants in NOD2 and IL23R modulates susceptibility to Crohn's disease.
    Török HP, Glas J, Endres I, Tonenchi L, Teshome MY, Wetzke M, Klein W, Lohse P, Ochsenkühn T, Folwaczny M, Göke B, Folwaczny C, Müller-Myhsok B, Brand S.
    Am J Gastroenterol; 2009 Jul; 104(7):1723-33. PubMed ID: 19455129
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  • 26. Association between genetic variants in the IL-23R gene and early-onset Crohn's disease: results from a case-control and family-based study among Canadian children.
    Amre DK, Mack D, Israel D, Morgan K, Lambrette P, Law L, Grimard G, Deslandres C, Krupoves A, Bucionis V, Costea I, Bissonauth V, Feguery H, D'Souza S, Levy E, Seidman EG.
    Am J Gastroenterol; 2008 Mar; 103(3):615-20. PubMed ID: 18047539
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  • 27. Autophagy gene ATG16L1 influences susceptibility and disease location but not childhood-onset in Crohn's disease in Northern Europe.
    Van Limbergen J, Russell RK, Nimmo ER, Drummond HE, Smith L, Anderson NH, Davies G, Gillett PM, McGrogan P, Weaver LT, Bisset WM, Mahdi G, Arnott ID, Wilson DC, Satsangi J.
    Inflamm Bowel Dis; 2008 Mar; 14(3):338-46. PubMed ID: 18088053
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  • 28. [Associations of Crohn's disease with DR4 and DR5 gene polymorphisms].
    Lin X, Jin L, Pan C, Zheng S, Zhang D, Lin X, Ding R, Jiang L, Jiang Y.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2015 Oct; 32(5):715-22. PubMed ID: 26418999
    [Abstract] [Full Text] [Related]

  • 29. ABCB1 3435C>T and 2677G>T/A polymorphisms in Polish and Bosnian patients with Crohn's disease - A preliminary report.
    Borecki K, Zawada I, Pawinska-Matecka A, Salkic NN, Karakiewicz B, Adler G.
    Bosn J Basic Med Sci; 2017 Nov 20; 17(4):323-327. PubMed ID: 28759738
    [Abstract] [Full Text] [Related]

  • 30. Smoking behaviour modifies IL23r-associated disease risk in patients with Crohn's disease.
    Doecke JD, Simms LA, Zhao ZZ, Roberts RL, Fowler EV, Croft A, Lin A, Huang N, Whiteman DC, Florin TH, Barclay ML, Merriman TR, Gearry RB, Montgomery GW, Radford-Smith GL.
    J Gastroenterol Hepatol; 2015 Feb 20; 30(2):299-307. PubMed ID: 24989722
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  • 38. Genetic factors conferring an increased susceptibility to develop Crohn's disease also influence disease phenotype: results from the IBDchip European Project.
    Cleynen I, González JR, Figueroa C, Franke A, McGovern D, Bortlík M, Crusius BJ, Vecchi M, Artieda M, Szczypiorska M, Bethge J, Arteta D, Ayala E, Danese S, van Hogezand RA, Panés J, Peña SA, Lukas M, Jewell DP, Schreiber S, Vermeire S, Sans M.
    Gut; 2013 Nov 20; 62(11):1556-65. PubMed ID: 23263249
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  • 39. Association of TNFSF15 polymorphisms in Korean children with Crohn's disease.
    Lee YJ, Kim KM, Jang JY, Song K.
    Pediatr Int; 2015 Dec 20; 57(6):1149-53. PubMed ID: 25998826
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